Product Details
- SNP ID
-
hCV90377386
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:100463188 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGGATTATGTTTCTTTCAAAGCCTT[C/G]TGTGTACATCTGTCTTTTCACCTGT
- Phenotype
-
MIM: 601396
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
WNT8B
PubMed Links
Gene Details
- Gene
- WNT8B
- Gene Name
- Wnt family member 8B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003393.3 |
134 |
Missense Mutation |
TCT,TGT |
S7C |
NP_003384.2 |
View Full Product Details